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Identification of a regulation network in response to cadmium toxicity using blood clam Tegillarca granosa as model
Clam, a filter-feeding lamellibranch mollusk, is capable to accumulate high levels of trace metals and has therefore become a model for investigation the mechanism of heavy metal toxification. In this study, the effects of cadmium were characterized in the gills of Tegillarca granosa during a 96-hou...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5071765/ https://www.ncbi.nlm.nih.gov/pubmed/27760991 http://dx.doi.org/10.1038/srep35704 |
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author | Bao, Yongbo Liu, Xiao Zhang, Weiwei Cao, Jianping Li, Wei Li, Chenghua Lin, Zhihua |
author_facet | Bao, Yongbo Liu, Xiao Zhang, Weiwei Cao, Jianping Li, Wei Li, Chenghua Lin, Zhihua |
author_sort | Bao, Yongbo |
collection | PubMed |
description | Clam, a filter-feeding lamellibranch mollusk, is capable to accumulate high levels of trace metals and has therefore become a model for investigation the mechanism of heavy metal toxification. In this study, the effects of cadmium were characterized in the gills of Tegillarca granosa during a 96-hour exposure course using integrated metabolomic and proteomic approaches. Neurotoxicity and disturbances in energy metabolism were implicated according to the metabolic responses after Cd exposure, and eventually affected the osmotic function of gill tissue. Proteomic analysis showed that oxidative stress, calcium-binding and sulfur-compound metabolism proteins were key factors responding to Cd challenge. A knowledge-based network regulation model was constructed with both metabolic and proteomic data. The model suggests that Cd stimulation mainly inhibits a core regulation network that is associated with histone function, ribosome processing and tight junctions, with the hub proteins actin, gamma 1 and Calmodulin 1. Moreover, myosin complex inhibition causes abnormal tight junctions and is linked to the irregular synthesis of amino acids. For the first time, this study provides insight into the proteomic and metabolomic changes caused by Cd in the blood clam T. granosa and suggests a potential toxicological pathway for Cd. |
format | Online Article Text |
id | pubmed-5071765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50717652016-10-26 Identification of a regulation network in response to cadmium toxicity using blood clam Tegillarca granosa as model Bao, Yongbo Liu, Xiao Zhang, Weiwei Cao, Jianping Li, Wei Li, Chenghua Lin, Zhihua Sci Rep Article Clam, a filter-feeding lamellibranch mollusk, is capable to accumulate high levels of trace metals and has therefore become a model for investigation the mechanism of heavy metal toxification. In this study, the effects of cadmium were characterized in the gills of Tegillarca granosa during a 96-hour exposure course using integrated metabolomic and proteomic approaches. Neurotoxicity and disturbances in energy metabolism were implicated according to the metabolic responses after Cd exposure, and eventually affected the osmotic function of gill tissue. Proteomic analysis showed that oxidative stress, calcium-binding and sulfur-compound metabolism proteins were key factors responding to Cd challenge. A knowledge-based network regulation model was constructed with both metabolic and proteomic data. The model suggests that Cd stimulation mainly inhibits a core regulation network that is associated with histone function, ribosome processing and tight junctions, with the hub proteins actin, gamma 1 and Calmodulin 1. Moreover, myosin complex inhibition causes abnormal tight junctions and is linked to the irregular synthesis of amino acids. For the first time, this study provides insight into the proteomic and metabolomic changes caused by Cd in the blood clam T. granosa and suggests a potential toxicological pathway for Cd. Nature Publishing Group 2016-10-20 /pmc/articles/PMC5071765/ /pubmed/27760991 http://dx.doi.org/10.1038/srep35704 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Bao, Yongbo Liu, Xiao Zhang, Weiwei Cao, Jianping Li, Wei Li, Chenghua Lin, Zhihua Identification of a regulation network in response to cadmium toxicity using blood clam Tegillarca granosa as model |
title | Identification of a regulation network in response to cadmium toxicity using blood clam Tegillarca granosa as model |
title_full | Identification of a regulation network in response to cadmium toxicity using blood clam Tegillarca granosa as model |
title_fullStr | Identification of a regulation network in response to cadmium toxicity using blood clam Tegillarca granosa as model |
title_full_unstemmed | Identification of a regulation network in response to cadmium toxicity using blood clam Tegillarca granosa as model |
title_short | Identification of a regulation network in response to cadmium toxicity using blood clam Tegillarca granosa as model |
title_sort | identification of a regulation network in response to cadmium toxicity using blood clam tegillarca granosa as model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5071765/ https://www.ncbi.nlm.nih.gov/pubmed/27760991 http://dx.doi.org/10.1038/srep35704 |
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